类阿片
阿片受体
受体
生物
药物发现
功能选择性
神经科学
信号转导
阿片肽
上瘾
计算生物学
G蛋白偶联受体
药理学
生物信息学
细胞生物学
生物化学
出处
期刊:Cell
[Elsevier]
日期:2023-11-01
卷期号:186 (24): 5203-5219
被引量:22
标识
DOI:10.1016/j.cell.2023.10.029
摘要
Opioids are used for pain management despite the side effects that contribute to the opioid crisis. The pursuit of non-addictive opioid analgesics remains unattained due to the unresolved intricacies of opioid actions, receptor signaling cascades, and neuronal plasticity. Advancements in structural, molecular, and computational tools illuminate the dynamic interplay between opioids and opioid receptors, as well as the molecular determinants of signaling pathways, which are potentially interlinked with pharmacological responses. Here, we review the molecular basis of opioid receptor signaling with a focus on the structures of opioid receptors bound to endogenous peptides or pharmacological agents. These insights unveil specific interactions that dictate ligand selectivity and likely their distinctive pharmacological profiles. Biochemical analysis further unveils molecular features governing opioid receptor signaling. Simultaneously, the synergy between computational biology and medicinal chemistry continues to expedite the discovery of novel chemotypes with the promise of yielding more efficacious and safer opioid compounds.
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